ライフサイエンスコーパス: architecturally

1 omal fibroblasts promotes the assembly of an architecturally abnormal ECM that is permissive to breas

2 rminal half of Hof1 displays misoriented and architecturally altered cables, along with impaired secr

3 doplasmic reticulum, present a rich array of architecturally and compositionally complex supramolecul

4 istinct subcellular compartments that differ architecturally and electrically.

5 Many Gram-negative pathogens assemble architecturally and functionally diverse adhesive pili o

6 e-mapped enhancers across the lineage-differ architecturally and functionally from low-complexity gen

7 f this complex interaction, a mature kidney, architecturally and functionally ready for extrauterine

8 eukaryotes, and that the terminin complex is architecturally and functionally similar to shelterin.

9 Individual cell types are defined by architecturally and functionally specialized cortical do

10 ns) of both gyrases are highly similar, both architecturally and in their ability to introduce writhe

11 Fully matured dental enamel is an architecturally and mechanically complex hydroxyapatite-

12 ave recently suggested that there may be two architecturally (and evolutionarily) distinct cognitive

13 ignment of the absolute configuration of the architecturally challenging compound (+)-scholarisine A

14 erpenoid alkaloids comprise some of the most architecturally complex and functional-group-dense secon

15 ant pathogen Agrobacterium tumefaciens forms architecturally complex biofilms on inert surfaces.

16 Bacillus subtilis is able to form architecturally complex biofilms on solid medium due to

17 ndomesticated strains such as NCIB 3610 form architecturally complex biofilms.

18 veloped viruses, the physical constraints of architecturally complex capsid viruses have imposed prac

19 ns are nonenveloped particles containing two architecturally complex capsids.

20 Bacteria form architecturally complex communities known as biofilms in

21 of Bacillus subtilis are capable of forming architecturally complex communities of cells known as bi

22 ium Bacillus subtilis are capable of forming architecturally complex communities of cells.

23 e such characteristic is the ability to form architecturally complex communities, referred to as biof

24 formation is coupled to the formation of an architecturally complex community of cells.

25 The total synthesis of the architecturally complex Daphniphyllum alkaloid (-)-calyc

26 minating in the first total synthesis of the architecturally complex daphniphyllum alkaloid, (-)-caly

27 gral membrane proteins within their immense, architecturally complex dendritic arbors.

28 ly believed and may facilitate expression of architecturally complex genes.

29 de of tryptamines with enol lactones to form architecturally complex heterocycles in high enantiomeri

30 A convergent total synthesis of the architecturally complex indole diterpenoid (-)-nodulispo

31 In the context of the synthesis of the architecturally complex Lycopodium alkaloid lyconadin A,

32 f posttranslational modifications to produce architecturally complex macrocyclic scaffolds.

33 ed total synthesis of (+)-tedanolide (1), an architecturally complex marine antitumor macrolide, has

34 ent, stereocontrolled total synthesis of the architecturally complex marine sponge metabolite (-)-eni

35 nents that are required for the formation of architecturally complex mature biofilms in these bacteri

36 nthetic gene clusters (BGCs), which assemble architecturally complex molecules from simple building b

37 ityl migration, Michael reaction) leading to architecturally complex molecules.

38 ketide synthesis to produce some of the most architecturally complex natural lipids including the ess

39 sformations allowed the construction of this architecturally complex natural product in significant q

40 ynthesis of organic compounds, especially of architecturally complex natural products, are not easily

41 The lung is an architecturally complex organ comprising a heterogeneous

42 des are a class of natural products that are architecturally complex potent antibiotics but generally

43 Microfabrication can create architecturally complex scaffolds for 3D cell cultures t

44 identifying strategies for the syntheses of architecturally complex secondary metabolites.

45 defines highly ordered myofiber patterns in architecturally complex tissue.

46 ent, stereocontrolled total synthesis of the architecturally complex tremorgenic indole alkaloid (-)-

47 ble to form a 4-fold symmetric complex that, architecturally, comprises two major substructures, a la

48 e, confirming that the hantaviral Gn fold is architecturally conserved across hantavirus clades.

49 Architecturally conserved viral portal dodecamers are ce

50 daily time course of radiation profiles for architecturally contrasting field-grown wheat (Triticum

51 ill allow for an easy and rapid synthesis of architecturally controlled supramolecular polymeric asse

52 nding of the histone-like protein, HU, to an architecturally critical position on DNA to facilitate t

53 some, further stabilized by HU binding to an architecturally critical position on the DNA.

54 d that the inhibitor selectively binds at an architecturally critical region of the protein.

55 Architecturally defective, leaky blood vessels typify pa

56 rt a semiautomated synthesis of sequence and architecturally defined, unimolecular macromolecules thr

57 These TOG4 structures architecturally depart from the structures of TOG domain

58 nto the tolerance and specificity of several architecturally different polyketide synthases.

59 of (-)-maoecrystal Z, demonstrate that three architecturally distinct ent-kauranoids can be prepared

60 rin-A5-EphB2 complex is a heterodimer and is architecturally distinct from the tetrameric EphB2-ephri

61 nocrystals and will enable the design of new architecturally distinct nanostructures.

62 ion of PAH involves major domain motions and architecturally distinct PAH tetramers.

63 l structures, it is not always clear whether architecturally distinct regions of the brain correspond

64 d bioinformatic analysis the existence of an architecturally distinct subfamily of acyl coenzyme A (a

65 tic fidelity and support our hypothesis that architecturally distinct TOGs arranged in a sequence-spe

66 opose an association of these modes with two architecturally distinct yet spatially overlapping and d

67 designed that present sequence diversity in architecturally distinct, biologically relevant combinat

68 t of actin nucleation factors that can build architecturally diverse actin structures.

69 The development of over 26 of these architecturally diverse adhesive organelles in various G

70 rescence spectroscopy has been used to probe architecturally diverse and unique model oligomers conta

71 ted high-avidity CD8 T cell populations with architecturally diverse clonotypic repertoires that disp

72 alkaloid (-)-205B, a tricyclic member of the architecturally diverse family of natural products isola

73 Examining embolism-induced failure of architecturally diverse leaf networks, we found that con

74 at species-rich ecological networks are more architecturally diverse than previously recognized.

75 These proteins are architecturally diverse, yet many of them share a conser

76 t wheat (Triticum aestivum) lines, which are architecturally diverse.

77 Centralized silos of genomic data are architecturally easier to initially design, develop and

78 Whether these TOG domains are architecturally equivalent is unknown.

79 reated tumors developed segmentally dilated, architecturally erratic tumor vessels with decreased nas

80 of memory storage is shown to occur both in architecturally feedforward networks and in recurrent ne

81 nding sites and the collagen-binding pocket, architecturally important hydrophobic residues and the h

82 nderstanding of this medically important and architecturally interesting portion of the genome, we ha

83 To address whether LTBP-1 functions architecturally like fibrillins, microfibrils were extra

84 d no detectable EPS(ETr) and did not form an architecturally mature biofilm.

85 re of bacteriophage genomes is that they are architecturally mosaic, with each individual genome repr

86 crocephaly is the consequence of a small but architecturally normal brain, and it is the cerebral cor

87 iption and splicing, result in a reduced but architecturally normal brain.

88 (fl/fl) conditional knockout (cKO) mice have architecturally normal brains and no gross behavioral de

89 truct neighboring Fz4(-/-) ECs to produce an architecturally normal mosaic vasculature, a cell nonaut

90 gh-resolution X-ray crystal structures of an architecturally novel aromatic PTase, Orf2 from Streptom

91 Marginal zones (MZs) are architecturally organized for clearance of and rapid res

92 Given that carboxysomes and architecturally related bacterial organelles are the sub

93 previously and in several unencountered with architecturally related benzyl ether-based supramolecula

94 leavage location can be conserved in distant architecturally related proteins.

95 unding member and its homologs FASTKD1-5 are architecturally related RNA-binding proteins, each havin

96 Although architecturally resembling voltage-gated ion channels, n

97 ectural diversification, where members of an architecturally rich ancestral community diversified the

98 inal winged helix DNA binding domain that is architecturally similar to that of the MarR family of tr

99 both the cerebellum and structures that are architecturally similar to the cerebellum.

100 ontains a core in the "ball-and-toes" region architecturally similar to the human U1 snRNP.

101 The Cmr complex is architecturally similar to the type I CRISPR-Cascade com

102 al superfamily members, although they may be architecturally similar, exhibit strict specificity towa

103 All BMCs share an architecturally similar, selectively permeable shell tha

104 The purpose of introns in the architecturally simple genome of Saccharomyces cerevisia

105 y cultured murine hippocampal neurons are an architecturally simple model for the study of cannabinoi

106 The architecturally stabilized closing of UDG enforces disto

107 It is well known that architecturally the brain is a neural network, i.e. a co

108 Architecturally, this complex shows striking resemblance

109 esults support the notion that LM and AL are architecturally, topographically, and connectionally dis

110 al polypeptides may be destroyed if they are architecturally unfit.

111 ructures developed that resembled lymphatics architecturally, were distinct from CD34-positive blood